Canonical Allele Identifier: CA5239696

Gene: HSPA5

Linked Data

• dbSNP Id: rs369271426
• ExAC: 9:128001145 A / G
• gnomAD v2: 9-128001145-A-G
• gnomAD v3: 9-125238866-A-G
• gnomAD v4: 9-125238866-A-G
• MyVariant Identifiers: chr9:g.128001145A>G (hg19) ; chr9:g.125238866A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238866A>G , CM000671.2:g.125238866A>G	GRCh38
NC_000009.11:g.128001145A>G , CM000671.1:g.128001145A>G	GRCh37
NC_000009.10:g.127040966A>G	NCBI36
NG_027761.1:g.7522T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-39T>C MANE Select	ENSP00000324173.6:n.997-39T>C
ENST00000679355.1:n.1313T>C
ENST00000679475.1:n.1581-39T>C
ENST00000680032.1:c.997-39T>C	ENSP00000506285.1:n.997-39T>C
ENST00000680234.1:n.1253-39T>C
ENST00000680257.1:n.1253-39T>C
ENST00000680272.1:c.996+75T>C	ENSP00000506097.1:n.996+75T>C
ENST00000680494.1:n.2382T>C
ENST00000680640.1:n.1948-39T>C
ENST00000681045.1:n.1877-39T>C
ENST00000681424.1:n.1313T>C
ENST00000681540.1:n.1253-39T>C
ENST00000681544.1:n.1328-39T>C
ENST00000681675.1:n.1877-39T>C
ENST00000681774.1:n.2219-39T>C
ENST00000324460.6:c.997-39T>C	ENSP00000324173.6:n.997-39T>C
NM_005347.4:c.997-39T>C	NP_005338.1:n.997-39T>C
NM_005347.5:c.997-39T>C MANE Select	NP_005338.1:n.997-39T>C